Katalyst Surgical, LLC

Katalyst Surgical, LLC — FDA 510(k) Submissions

Katalyst Surgical, LLC has submitted 7 FDA 510(k) premarket notifications since 2012, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laser, Ophthalmic, Electrosurgical, Cutting & Coagulation & Accessories, Illuminator, Fiberoptic, Surgical Field, Lens, Surgical, Laser, Accesssory, Ophthalmic Laser, Instrument, Ultrasonic Surgical . Use the specialty filter in the sidebar to narrow results.